Contemplating the Bone Marrow Transplant

Now that Zoe has stabilized and begun Chemotherapy, Michelle and I have started to think more critically about the Bone Marrow Transplant (BMT) that has been recommended. There are a number of problems to be tackled, and it really is a matter of life and death so it’s incumbent upon us as Zoe’s parents and advocates to do our best to make a good decision.

Here are the complicating factors, as best we know so far:

  • While Zoe is expected to survive chemo and see no long term problems from it, the BMT has a very high mortality rate should she be subjected to it: generally accepted to be 30%, as in, 30% of patients die from complications
  • BMT is the only cure for the Familial type of HLH, however it is not necessarily required to survive and thrive in the wake of acquired HLH
  • Determining if Zoe has FHLH is difficult and not 100%; we’ll do genetic testing and if she has the markers, we will know, however it is also possible for the marker to be “hidden” as I understand it, meaning doctors are likely to recommend a BMT no matter what just to be sure
  • There have been cases of children under 1 year of age who were indeterminant as to which type they had and who opted not to get the BMT and who still survive many years later with no symptoms of the disease remaining
  • In addition to the base mortality rate of the procedure, the side affects of complication to BMT can include both neurological and physical defects, meaning Zoe has a rather high chance of either dying or being left with lifelong mental or physical disabilities to contend with; the chemotherapy introduces none of these risks by itself.
  • If we are unable to determine if she has FHLH and opt not to do a BMT, there is a very high chance that if she turns out to have FHLH the disease could reemerge rapidly and a simple infection could in fact kill her before the disease can be put into remission again
  • At this point we are focused on getting Zoe through the first stages of Chemo and discussing these issues with Dr. M. We need to know a great deal more about the genetic testing and how sure we can be about the results — is it ever possible to know that a child does not have FHLH and instead has the acquired type? The answer to this will help us move toward a decision. We are very wary of the idea of putting Zoe back in harm’s way without being sure that there is a necessity, given that the BMT can be so very deadly.

4 thoughts on “Contemplating the Bone Marrow Transplant

  1. Pingback: Surgery & Etoposide : HLH Journal

  2. Pingback: The Transplant Decision : HLH Journal

  3. Thank you for this page. This is by far the hardest and most confusing thing I’ve faced in my life. My daughter is devastated!

  4. my son will be getting a bmt hopefully in september to treat his hlh and if my prayers are answered he will make a full recovery and go back to being the healthy, funny, crazy, cheeky child that i miss terribly. i will prayer for your daughter also and i truly know how hard this is for you and no matter what thing i say to you about staying positive your lives have been turned upside down and no doubt you will be fighting to keep it together and just make it through each day because i know that that is definitely the case for me. you are all in my thoughts and prayers and i wish you the best of luck x

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